| Product NDC: | 65224-615 |
| Proprietary Name: | Z-COF |
| Non Proprietary Name: | PSEUDOEPHEDRINE HYDROCHLORIDE, GUAIFENESIN, and DEXTROMETHORPHAN HYDROBROMIDE |
| Active Ingredient(s): | 15; 175; 30 mg/5mL; mg/5mL; mg/5mL & nbsp; PSEUDOEPHEDRINE HYDROCHLORIDE, GUAIFENESIN, and DEXTROMETHORPHAN HYDROBROMIDE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 65224-615 |
| Labeler Name: | Pernix Therapeutics |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20111117 |
| Package NDC: | 65224-615-16 |
| Package Description: | 473 mL in 1 BOTTLE (65224-615-16) |
| NDC Code | 65224-615-16 |
| Proprietary Name | Z-COF |
| Package Description | 473 mL in 1 BOTTLE (65224-615-16) |
| Product NDC | 65224-615 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | PSEUDOEPHEDRINE HYDROCHLORIDE, GUAIFENESIN, and DEXTROMETHORPHAN HYDROBROMIDE |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 20111117 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Pernix Therapeutics |
| Substance Name | DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PSEUDOEPHEDRINE HYDROCHLORIDE |
| Strength Number | 15; 175; 30 |
| Strength Unit | mg/5mL; mg/5mL; mg/5mL |
| Pharmaceutical Classes |